Variant report

Variant	rs10006350
Chromosome Location	chr4:124657333-124657334
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs12331302	1.00[AMR][1000 genomes]
rs28439631	1.00[AMR][1000 genomes]
rs28503204	1.00[AMR][1000 genomes]
rs28580374	1.00[AMR][1000 genomes]
rs28694275	1.00[AMR][1000 genomes]
rs28778663	1.00[AMR][1000 genomes]
rs28848525	1.00[AMR][1000 genomes]
rs28896233	1.00[AMR][1000 genomes]
rs58619925	1.00[AMR][1000 genomes]
rs59840299	1.00[AMR][1000 genomes]
rs6831187	1.00[AMR][1000 genomes]
rs72913221	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34581	chr4:124271321-125247395	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv830047	chr4:124504051-124699142	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:124651000-124666000	Weak transcription	Psoas Muscle	Psoas
2	chr4:124654400-124658200	Weak transcription	Fetal Intestine Small	intestine
3	chr4:124656200-124658800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr4:124657200-124657400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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